MCT4 mediates hypoxia-induced extracellular lactate release from IPF fibroblasts.

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Bibliographic Details
Title: MCT4 mediates hypoxia-induced extracellular lactate release from IPF fibroblasts.
Authors: Nho RS; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Nielsen L; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Roberts J; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Diep S; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Taylor A; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Hager K; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Yengo R; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Rosas L; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Farkas L; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Prasad J; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Mebratu YA; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Rojas M; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States., Chan SY; Department of Medicine, University of Pittsburgh, Pittsburgh, PA, United States., Horowitz JC; Division of Pulmonary, Department of Internal Medicine and The Davis Heart and Lung Research Institute, Critical Care and Sleep Medicine, The Ohio State University, Columbus, OH, United States.
Source: American journal of respiratory cell and molecular biology [Am J Respir Cell Mol Biol] 2026 Jul 01; Vol. 74 (7), pp. 924-935.
Publication Type: Journal Article
Journal Info: Publisher: American Thoracic Society Country of Publication: England NLM ID: 8917225 Publication Model: Print Cited Medium: Internet ISSN: 1535-4989 (Electronic) Linking ISSN: 10441549 NLM ISO Abbreviation: Am J Respir Cell Mol Biol Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1535-4989
DOI:10.1093/ajrcmb/aanag015